Stolc V
J Hered. 1984 Sep-Oct;75(5):414-5. doi: 10.1093/oxfordjournals.jhered.a109969.
The genetic heterogeneity of ceruloplasmin in serum was studied in the progeny of the (LEW X BN)F1 X (LEW X BN)F1 rats. The results of the statistical analysis showed that the Hbb and c loci were linked. However, the autosomal Ces gene was not linked to the Hbb or c loci. The Ces gene was expressed in normal Mendelian pattern and had two alleles that manifested a low (Cesl) or high (Cesh) level of the enzyme in serum. The Cesl gene was expressed as a dominant in the F1 generation. Two phenotypes CES-H and CES-L were found in the F2 rats; the females in the parental strain and hybrid had higher ceruloplasmin concentration than the male rats.
在(LEW×BN)F1×(LEW×BN)F1大鼠的子代中研究了血清铜蓝蛋白的遗传异质性。统计分析结果表明,Hbb和c位点是连锁的。然而,常染色体Ces基因与Hbb或c位点不连锁。Ces基因以正常孟德尔模式表达,有两个等位基因,在血清中表现出低(Cesl)或高(Cesh)水平的酶。Cesl基因在F1代中呈显性表达。在F2大鼠中发现了两种表型CES-H和CES-L;亲本品系和杂种中的雌性大鼠铜蓝蛋白浓度高于雄性大鼠。